Positional specialization of LIR motifs in RavZ and the autophagy-related protein ATG4B

LC3-interacting region (LIR) motifs are essential for recruiting proteins onto autophagosomes, the hallmark of autophagy. We recently explored the relevance of the specific position of the LIRs in RavZ and ATG4B (autophagy-related 4B). RavZ's N-terminal LIRs drive substrate recognition and enzymatic activity, while its C-terminal LIR aids membrane localization. In contrast, ATG4B's C-terminal LIR is indispensable for LC3B (microtubule-associated protein 1 light chain 3B)-phosphatidylethanolamine (PE) delipidation on autophagosomes but not required for cytosolic LC3B priming, which is mediated solely by its catalytic domain (CAD). These findings underscore the structural adaptation of LIRs for context-specific functions. This novel nuanced understanding provides a framework for developing therapeutic tools to modulate autophagy by precisely targeting LIRs or their associated processes, offering potential treatment for diseases like neurodegenerative disorders and infections characterized by autophagy dysregulation.

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Publication Details

Journal
Autophagy Reports
Published
2024-12-19
DOI
https://doi.org/10.1080/27694127.2024.2438563
Citations
1
Primary Topic
Autophagy in Disease and Therapy
Type
article
Field-Weighted Citation Impact
0.39

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article

Positional specialization of LIR motifs in RavZ and the autophagy-related protein ATG4B

Sang-Won Park, Deok-Jin Jang, Jin‐A Lee
1 citations
Autophagy Reports
Autophagy in Disease and Therapy
0.39
article

Positional specialization of LIR motifs in RavZ and the autophagy-related protein ATG4B

Sang-Won Park, Deok-Jin Jang, Jin‐A Lee
article en
1 citations

Abstract

LC3-interacting region (LIR) motifs are essential for recruiting proteins onto autophagosomes, the hallmark of autophagy. We recently explored the relevance of the specific position of the LIRs in RavZ and ATG4B (autophagy-related 4B). RavZ's N-terminal LIRs drive substrate recognition and enzymatic activity, while its C-terminal LIR aids membrane localization. In contrast, ATG4B's C-terminal LIR is indispensable for LC3B (microtubule-associated protein 1 light chain 3B)-phosphatidylethanolamine (PE) delipidation on autophagosomes but not required for cytosolic LC3B priming, which is mediated solely by its catalytic domain (CAD). These findings underscore the structural adaptation of LIRs for context-specific functions. This novel nuanced understanding provides a framework for developing therapeutic tools to modulate autophagy by precisely targeting LIRs or their associated processes, offering potential treatment for diseases like neurodegenerative disorders and infections characterized by autophagy dysregulation.

Autophagy ReportsVol. 4(1)
Hannam University (KR), Kyungpook National University (KR)
Ministry of Science and ICT, South Korea
Good health and well-being
Openalex Percentile: Top 31%
Autophagy in Disease and Therapy
0.39
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Positional specialization of LIR motifs in RavZ and the autophagy-related protein ATG4B — Sang-Won Park, Deok-Jin Jang, et al. · Autophagy Reports (2024) | TGRS Research Map | TGRS